enalapril maleate and hydrochlorothiazide (51672-4046)

Drug Facts

Product Profile

Brand Name enalapril maleate and hydrochlorothiazide

Generic Name enalapril maleate and hydrochlorothiazide

Labeler taro pharmaceuticals u.s.a., inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

enalapril maleate 10 mg/1, hydrochlorothiazide 25 mg/1

Manufacturer

Taro Pharmaceuticals U.S.A., Inc.

Identifiers & Regulatory

Product NDC 51672-4046

Product ID 51672-4046_1130a62d-94e3-2dc6-e063-6394a90a8a67

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA075788

Listing Expiration 2026-12-31

Marketing Start 2001-09-18

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724046

Hyphenated Format 51672-4046

Supplemental Identifiers

RxCUI

858824 858828

UNII

0J48LPH2TH 9O25354EPJ

NUI

N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name enalapril maleate and hydrochlorothiazide (source: ndc)

Generic Name enalapril maleate and hydrochlorothiazide (source: ndc)

Application Number ANDA075788 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1
25 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (51672-4046-1)
1000 TABLET in 1 BOTTLE (51672-4046-3)

source: ndc

Packages (2)

51672-4046-1 100 TABLET in 1 BOTTLE (51672-4046-1) 51672-4046-3 1000 TABLET in 1 BOTTLE (51672-4046-3)

Ingredients (2)

enalapril maleate (10 mg/1) hydrochlorothiazide (25 mg/1)

Linked Drug Pages (1)

Enalapril Maleate and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "1130a62d-94e3-2dc6-e063-6394a90a8a67", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "9O25354EPJ"], "rxcui": ["858824", "858828"], "spl_set_id": ["7cb92cf2-46f2-4379-937c-168d230e43a4"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4046-1)", "package_ndc": "51672-4046-1", "marketing_start_date": "20010918"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (51672-4046-3)", "package_ndc": "51672-4046-3", "marketing_start_date": "20010918"}], "brand_name": "Enalapril Maleate and Hydrochlorothiazide", "product_id": "51672-4046_1130a62d-94e3-2dc6-e063-6394a90a8a67", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51672-4046", "generic_name": "Enalapril Maleate and Hydrochlorothiazide", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate and Hydrochlorothiazide", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA075788", "marketing_category": "ANDA", "marketing_start_date": "20010918", "listing_expiration_date": "20261231"}